Canonical Allele Identifier: CA381569220

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1169393051
• MyVariant Identifiers: chr11:g.67803796G>A (hg19) ; chr11:g.68036329G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036329G>A , CM000673.2:g.68036329G>A	GRCh38
NC_000011.9:g.67803796G>A , CM000673.1:g.67803796G>A	GRCh37
NC_000011.8:g.67560372G>A	NCBI36
NG_007878.1:g.2314G>A , LRG_115:g.2314G>A
NG_017040.1:g.10713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.449G>A MANE Select	ENSP00000315774.5:p.Cys150Tyr
ENST00000313468.9:c.449G>A	ENSP00000315774.5:p.Cys150Tyr
ENST00000524810.5:c.381G>A
ENST00000525419.5:c.395G>A	ENSP00000433521.1:p.Cys132Tyr
ENST00000526339.5:c.449G>A	ENSP00000436287.1:p.Cys150Tyr
ENST00000526446.5:c.*504G>A	ENSP00000433645.1:n.*504G>A
ENST00000528492.1:c.11G>A	ENSP00000432848.1:p.Cys4Tyr
ENST00000531282.1:n.301G>A
NM_002496.3:c.449G>A	NP_002487.1:p.Cys150Tyr
XM_005274013.1:c.449G>A	XP_005274070.1:p.Cys150Tyr
XM_005274014.1:c.449G>A	XP_005274071.1:p.Cys150Tyr
XM_005274015.1:c.329G>A	XP_005274072.1:p.Cys110Tyr
XM_011545053.1:c.449G>A	XP_011543355.1:p.Cys150Tyr
NM_002496.4:c.449G>A MANE Select	NP_002487.1:p.Cys150Tyr